A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738117



Internal ID161783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154460917..154460973hg38UCSC Ensembl
chrX:153689257..153689313hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416970
Supporting Variants
Samples
Known GenesPLXNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738117
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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